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Repeated-dose liver and gastrointestinal tract micronucleus assays with CI Solvent Yellow 14 (Sudan I) using young adult rats.
- Source :
-
Mutation research. Genetic toxicology and environmental mutagenesis [Mutat Res Genet Toxicol Environ Mutagen] 2015 Mar; Vol. 780-781, pp. 76-80. Date of Electronic Publication: 2014 Sep 16. - Publication Year :
- 2015
-
Abstract
- The in vivo genotoxicity of CI Solvent Yellow 14 (Sudan I) was examined using repeated-dose liver and gastrointestinal tract micronucleus (MN) assays in young adult rats. Sudan I is a mono-azo dye based on aniline and 1-amino-2-hydroxynaphthalene. This dye was demonstrated as a rat liver carcinogen in a National Toxicology Program (NTP) bioassay, and genotoxicity was noted in a rat bone marrow micronucleus (BMMN) assay. In the present study, Sudan I was administered orally to rats for 14-days, and the MN frequency in the liver, stomach, colon, and bone marrow were analyzed. The frequency of micronucleated hepatocytes (MNHEPs) was not significantly increased by the administration of the Sudan I. Gastrointestinal tract MNs were also not induced. However, in the BMMN assay, a significant increase in micronucleated immature erythrocytes (MNIMEs) was observed in a dose-dependent manner. While Sudan I has been reported to lack hepatic genotoxicity, it has also exhibited tumor-promoting activities. These results are consistent with the lack of induction of MN in the hepatocytes. The lack of MN induction in cells of the gastrointestinal tract was also logical because azo-compounds are reported to be unlikely to induce DNA damage in the rat gut. The repeated-dose rat liver and gastrointestinal tract MN assays have the potential to be used in the evaluation of the genotoxicity of a chemical in each organ in accordance with its mode of action.<br /> (Copyright © 2014. Published by Elsevier B.V.)
- Subjects :
- Administration, Oral
Age Factors
Animals
Body Weight drug effects
Bone Marrow pathology
Chromosome Aberrations drug effects
Colon drug effects
Cooperative Behavior
Dose-Response Relationship, Drug
Drug Administration Schedule
Hepatocytes drug effects
Humans
Japan
Liver drug effects
Male
Organ Specificity
Rats
Rats, Sprague-Dawley
Reticulocytes pathology
Societies, Pharmaceutical
Stomach drug effects
Bone Marrow drug effects
Carcinogens toxicity
Micronucleus Tests
Naphthols toxicity
Reticulocytes drug effects
Subjects
Details
- Language :
- English
- ISSN :
- 1879-3592
- Volume :
- 780-781
- Database :
- MEDLINE
- Journal :
- Mutation research. Genetic toxicology and environmental mutagenesis
- Publication Type :
- Academic Journal
- Accession number :
- 25892626
- Full Text :
- https://doi.org/10.1016/j.mrgentox.2014.09.002